The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
88626322 8862632 2 F 20100304 20160908 20121026 20160915 EXP US-MERCK-1210USA006484 MERCK 0.00 F Y 0.00000 20160915 MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
88626322 8862632 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW 20560 70 MG TABLET /wk
88626322 8862632 2 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, QW 0 70 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
88626322 8862632 1 Osteoporosis
88626322 8862632 2 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
88626322 8862632 OT
88626322 8862632 DS
88626322 8862632 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
88626322 8862632 Ankle fracture
88626322 8862632 Anxiety
88626322 8862632 Death
88626322 8862632 Depression
88626322 8862632 Fall
88626322 8862632 Femur fracture
88626322 8862632 Leukaemia
88626322 8862632 Sternal fracture

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
88626322 8862632 1 20031104 200802 0
88626322 8862632 2 20080228 201003 0